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Author Correction: Inherent mosaicism and extensive mutation of human placentas.
Coorens, Tim H H; Oliver, Thomas R W; Sanghvi, Rashesh; Sovio, Ulla; Cook, Emma; Vento-Tormo, Roser; Haniffa, Muzlifah; Young, Matthew D; Rahbari, Raheleh; Sebire, Neil; Campbell, Peter J; Charnock-Jones, D Stephen; Smith, Gordon C S; Behjati, Sam.
Afiliação
  • Coorens THH; Wellcome Sanger Institute, Hinxton, UK.
  • Oliver TRW; Wellcome Sanger Institute, Hinxton, UK.
  • Sanghvi R; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Sovio U; Wellcome Sanger Institute, Hinxton, UK.
  • Cook E; Department of Obstetrics and Gynaecology, University of Cambridge, NIHR Cambridge Biomedical Research Centre, Cambridge, UK.
  • Vento-Tormo R; Department of Obstetrics and Gynaecology, University of Cambridge, NIHR Cambridge Biomedical Research Centre, Cambridge, UK.
  • Haniffa M; Wellcome Sanger Institute, Hinxton, UK.
  • Young MD; Wellcome Sanger Institute, Hinxton, UK.
  • Rahbari R; Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
  • Sebire N; Department of Dermatology, Royal Victoria Infirmary, Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
  • Campbell PJ; Wellcome Sanger Institute, Hinxton, UK.
  • Charnock-Jones DS; Wellcome Sanger Institute, Hinxton, UK.
  • Smith GCS; Great Ormond Street Hospital for Children NHS Foundation Trust, NIHR Great Ormond Street Hospital Biomedical Research Centre, London, UK.
  • Behjati S; UCL Great Ormond Street Institute of Child Health, London, UK.
Nature ; 603(7901): E17, 2022 Mar.
Article em En | MEDLINE | ID: mdl-35228729

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nature Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nature Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido